Join Max's team and help add tomorrows!
This is the fifth aniversary of Team MAXpedition! Thank you over and over to everyone that continues to support the CF Foundation and Team MAXpedition each year.
For anyone not familiar with why this is so important to us: Our son Max (4yo) was diagnosed with Cystic Fibrosis 2 weeks after birth. He spends over an hour doing respiratory therapy treatments and takes an insane amount of medications each day (~20 pills, 2 nebulizers, 3 liquid meds, and Orkambi). CF is considered a rare genetic disorder so we rely heavily on research that is funded by the Cystic Fibrosis Foundation to search for effective treatments and one day a cure.
Max is one of approximately of 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day just to breathe. We walk for them. Will you join us? To become a member of our team, just click on the "Join our Team" button. From there you can make a donation and start your fundraising.
By becoming a member and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Jen and Shaun
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: